Results 181 to 190 of about 131,131 (300)

Predictive value of neutrophil-to-lymphocyte ratio and fibrinogen degradation products for renal involvement in pediatric immunoglobulin A vasculitis. [PDF]

Transl Pediatr
Li G, Liao J, Zhan Z, Zeng J, Su D.
europepmc   +1 more source

SLE Presenting With Unilateral Loculated Pleural Effusion in a Young Hypertensive Female: A Rare Case Report and Literature Review

Clinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT SLE can rarely present with unilateral pleural effusion or hypertension. A 28‐year‐old woman with loculated exudative pleural effusion was diagnosed with SLE and lupus nephritis fulfilling EULAR/ACR criteria, treated with pigtail drainage, corticosteroids, and hydroxychloroquine, with good recovery.
Amrit Tripathi, Ujwal Sah, Saurav Shah, Shivaditya Singh, Surya Raj Nishad   +4 more
wiley   +1 more source

A Case of Hereditary Angioedema Types I/II That Successfully Achieved Pregnancy and Delivery After Infertility Treatment. [PDF]

J Dermatol
Ohzono A, Maeda S, Koga H, Nakama T.
europepmc   +1 more source

Hydrocephalus and Diffuse Alveolar Hemorrhage as the Initial Manifestation of Systemic Lupus Erythematosus and Antiphospholipid Syndrome: A Case Report

Clinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Systemic lupus erythematosus (SLE) is an autoimmune disease that can affect many systems, such as the central nervous system (CNS), cardiovascular, musculocutaneous, renal, and respiratory systems, etc. SLE can occur alone or in association with other autoimmune diseases, especially antiphospholipid syndrome (APS).
Ehsan Adib, Narges Gorbanmaleki, Amirreza Eterafi, Sara Jalali Jivan   +3 more
wiley   +1 more source

Genetic kidney diseases - from discovery to precision care. [PDF]

Med Genet
Simons M, Hoefele J.
europepmc   +1 more source

Inherited microcytic anemias due to disorders of iron and heme metabolism: An updated clinical review

HemaSphere, Volume 10, Issue 9, September 2026.
Abstract Microcytic anemia is among the most common hematological abnormalities in clinical practice and is usually attributable to iron deficiency, thalassemia traits, or anemia of inflammation. A small but clinically important subset of patients, however, has inherited disorders of iron metabolism or heme synthesis presenting with persistent ...
Alexandros Makis, Ioanna Saougou, Eleftheria Hatzimichael   +2 more
wiley   +1 more source

Genetic heterogeneity correlated with phenotypic variability in 6 Chinese families with Alport syndrome. [PDF]

Front Genet
Gao J, Zhou H, Zhang L, Su Z, Liu S.
europepmc   +1 more source

PPI Misuse in Bangladesh: Confronting a Silent Epidemic Through Deprescribing and Regulatory Reform—A Policy Perspective

Health Science Reports, Volume 9, Issue 9, September 2026.
ABSTRACT Background and Aims Proton pump inhibitors (PPIs) are subject to rampant global misuse, posing a significant public health challenge. This issue is particularly acute in low‐ and middle‐income countries like Bangladesh, where preliminary data indicate alarmingly high rates of inappropriate prescribing, driven by systemic factors within the ...
Abdullaha Al Mamun, Md Rabiul Awual, K. A. M. Inzamul Islam   +2 more
wiley   +1 more source

From Sight to Stridor: Recurrent Angioedema in Systemic Lupus Erythematosus Associated With Complement Activation. [PDF]

Am J Case Rep
Khalafi S, Felde L.
europepmc   +1 more source

When Blood Proteins Reveal What Transcripts Miss: Immune Cell Priming and the Road to Prognostic Biomarkers in Lupus

Arthritis &Rheumatology, Volume 78, Issue 9, Page 1823-1825, September 2026.
Ioannis Parodis
wiley   +1 more source